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95450-80-9

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95450-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95450-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,4,5 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95450-80:
(7*9)+(6*5)+(5*4)+(4*5)+(3*0)+(2*8)+(1*0)=149
149 % 10 = 9
So 95450-80-9 is a valid CAS Registry Number.

95450-80-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetic acid, 2-(2,5-dimethylphenoxy)-, methyl ester

1.2 Other means of identification

Product number -
Other names Acetic acid, (2,5-dimethylphenoxy)-, methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:95450-80-9 SDS

95450-80-9Relevant articles and documents

Preparation method of anti-proliferation reactive intermediate ML-098

-

Paragraph 0011; 0020-0021, (2018/10/04)

The invention discloses a preparation method of an anti-proliferation reactive intermediate ML-098 with the chemical name of 1-(2-(2,5-dimethyl phenoxy)ethyl)-3-indolecarboxylic acid, and belongs to the field of a chemical medicine intermediate. The metho

Captodative olefins: Methyl 2-aryloxy-3-dimethyl-aminopropenoates and their application in a new synthesis of benzofurans

Cruz, María Del Carmen,Tamariz, Joaquín

, p. 2377 - 2380 (2007/10/03)

The β-substituted captodative olefins methyl 2-aryloxy-3- dimethylaminopropenoates 4a-h were synthesized, via aminomethylenation of the corresponding 2-phenoxyacetic esters 9a-h. Lewis acid promoted intramolecular cyclization of alkenes 4 led to benzofurans 7a-h, in an efficient synthetic approach to the benzofuran frame.

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